CE Marking is also known as CE mark. CE marking certification is a mandatory to export products to Euerop. With the CE marking on a product the manufacturer ensures that the product is in conformity with the essential requirements of the applicable EC directives. The letters “CE” stand for “Conformité Européenne” (“European Conformity”).
Depending on the level of risk of the product, the CE Mark is affixed to a product by the manufacturer or authorized representative after ensuring that the product meets all the CE mark requirements. CE Mark can be notified or non-notified.
Ensures machinery’s safety by setting essential health and safety requirements for design, construction, and operation.
Applies to electrical equipment within certain voltage limits, ensuring it’s safe to use.
Ensures electromagnetic compatibility of electrical and electronic equipment to prevent interference with other devices.
Regulates medical devices to ensure their safety, quality, and performance.
Restricts the use of hazardous substances in electrical and electronic equipment to protect human health and the environment.
Sets requirements for personal protective equipment to protect users against risks to health and safety.
Ensures the free movement of pressure equipment within the EU market by setting safety requirements.
Regulates equipment intended for use in potentially explosive atmospheres to ensure safety.
Ensures toys meet safety standards to protect children’s health and safety.
Establishes harmonized conditions for the marketing of construction products to ensure their performance and safety.
Sets requirements for placing radio equipment on the market to ensure its compatibility and efficient use of radio spectrum.
Applies to appliances burning gaseous fuels to ensure their safety and proper functioning.
Ensures the conformity of measuring instruments used for commercial transactions, safety, and health protection.
Regulates the marketing of pyrotechnic articles to ensure their safe use.
Applies to weighing instruments used for commercial transactions, ensuring their accuracy and reliability.
Sets requirements for the design, manufacturing, and conformity assessment of simple pressure vessels.
Regulates in vitro diagnostic medical devices to ensure their safety and reliability.
Applies to marine equipment to ensure its safety, environmental protection, and quality.
Establishes noise emission limits for outdoor equipment to protect the environment and public health.
Sets requirements for personal watercraft to ensure their safety and environmental protection.
Regulates active implantable medical devices to ensure their safety and performance.
Regulates the placing on the market of explosives for civil uses to ensure their safe handling and use.
Sets requirements for the manufacture, placing on the market, and use of civil explosives.
Establishes a system for the notification and monitoring of incidents involving medical devices.
Regulates the placing on the market and use of biocidal products to ensure their effectiveness and safety.
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